ZMP

zgc:136461

Ensembl ID:

ENSDARG00000093844

ZFIN ID:

ZDB-GENE-060519-7

Description:

hypothetical protein LOC562139 [Source:RefSeq peptide;Acc:NP_001075159]

Human Orthologues:

CTRB1, CTRB2

Human Descriptions:

chymotrypsinogen B1 [Source:HGNC Symbol;Acc:2521]
chymotrypsinogen B2 [Source:HGNC Symbol;Acc:2522]

Mouse Orthologue:

Ctrb1

Mouse Description:

chymotrypsinogen B1 Gene [Source:MGI Symbol;Acc:MGI:88559]

Alleles

There are 5 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa11393	Nonsense	Available for shipment	Available now
sa25368	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa34120	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa11393

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
Order Allele From EZRC

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000022139	Nonsense	48	263	2	7

The following genes are also affected by this mutation:

ENSDARG00000090428

Genomic Location (Zv9):

Chromosome 7 (position 36522967)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	34796810
GRCz11	7	35068287

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ATGCCAGGATTGTRAACGGTGAGGAGGCTGTCCCTCATTCCTGGCCCTGG[C/T]AGGTGTCTCTGCAGRTATGAAYAGACAGATTTTCACTTACAGATGACATT

Long Flanking Sequence:

GTCATTTGTTTGAGATGAAATGCATAATATATATTCCACTTTTATGAAATCATGTCCATGAAATATGACAGACCTTCTTCCGATACAATTAGCTCCTGCAAGTGTTAGCAATAACAAGTGACACGTACAGCTAAAAGTGCTCAAAGTACTCAATGGAAAGTCAGCAAATTCTGAGAATGAGAATGTTGCAAAATATGTAAATAAGCAGGAAGGTCAGATATATAAACCCCTCGAGTTGGTGAGACATTGGTGACTCAGAAATGGCTTTCGTCTGGATTTTGTCGTGCCTTGCCTTGATTGGAACAGCATATGGTAAATTGCTGATTTTTTCCCTCTTATTTAACAATTTGAATGAATGTGTCCCACTTTGATTTATATAAAAATTTTAACAAGTGCTTTTTTATTCTGAAGGCTGTGGCGTTCCTGCCATCCCTCCTGTTATTACCGGTTATGCCAGGATTGTAAACGGTGAGGAGGCTGTCCCTCATTCCTGGCCCTGG[C/T]AGGTGTCTCTGCAGGTATGAACAGACAGATTTTCACTTACAGATGACATTAGGATAGGCAACTGTGAATAAAAAAATTGATCTGATGTTTAATGTAAGGACTCCACCGGCTTCCACTTCTGCGGAGGCTCCCTGATCAACGAGTGGTGGGTTGTGACTGCTGCTCACTGCAACGTCAGGTAAGACAGCATTGACGCTTTGTTTCTCCATCATGCAATGAATTTAAGACGTATGTGCAAATTTGAGAGTAAAATAGTCAAATCTTTTTATTAGGACCTCTCACCGTGTCATCCTGGGTGAGCATGATCGTTCCTCCAATGCTGAGCCCATTCAGACCATGACCGTTGGAAAGGTATGGTGAACTCTAAAAAATGCTAGGTCATTGTTACTCCATGTTGGGTCAAATTTAGATAAATCCAACAGTTGGGTTAAAACGTGTCATTTACATGGTTTAAATGTTGGGTTTGTCCATATTTAACCCAATGCTGGGTTAGGACAAAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa25368

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000022139	Essential Splice Site	53	263	None	7

The following genes are also affected by this mutation:

ENSDARG00000090428

Genomic Location (Zv9):

Chromosome 7 (position 36523064)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	34796907
GRCz11	7	35068384

KASP Assay ID:

554-7835.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CATTAGGATAGGCAACTGTGAATAAAAAAATTGATCTGATGTTTAATGTA[A/G]GGACTCCACCGGCTTCCACTTCTGCGGAGGCTCCCTGATCAACGAGTGGT

Long Flanking Sequence:

GCAAGTGTTAGCAATAACAAGTGACACGTACAGCTAAAAGTGCTCAAAGTACTCAATGGAAAGTCAGCAAATTCTGAGAATGAGAATGTTGCAAAATATGTAAATAAGCAGGAAGGTCAGATATATAAACCCCTCGAGTTGGTGAGACATTGGTGACTCAGAAATGGCTTTCGTCTGGATTTTGTCGTGCCTTGCCTTGATTGGAACAGCATATGGTAAATTGCTGATTTTTTCCCTCTTATTTAACAATTTGAATGAATGTGTCCCACTTTGATTTATATAAAAATTTTAACAAGTGCTTTTTTATTCTGAAGGCTGTGGCGTTCCTGCCATCCCTCCTGTTATTACCGGTTATGCCAGGATTGTAAACGGTGAGGAGGCTGTCCCTCATTCCTGGCCCTGGCAGGTGTCTCTGCAGGTATGAACAGACAGATTTTCACTTACAGATGACATTAGGATAGGCAACTGTGAATAAAAAAATTGATCTGATGTTTAATGTA[A/G]GGACTCCACCGGCTTCCACTTCTGCGGAGGCTCCCTGATCAACGAGTGGTGGGTTGTGACTGCTGCTCACTGCAACGTCAGGTAAGACAGCATTGACGCTTTGTTTCTCCATCATGCAATGAATTTAAGACGTATGTGCAAATTTGAGAGTAAAATAGTCAAATCTTTTTATTAGGACCTCTCACCGTGTCATCCTGGGTGAGCATGATCGTTCCTCCAATGCTGAGCCCATTCAGACCATGACCGTTGGAAAGGTATGGTGAACTCTAAAAAATGCTAGGTCATTGTTACTCCATGTTGGGTCAAATTTAGATAAATCCAACAGTTGGGTTAAAACGTGTCATTTACATGGTTTAAATGTTGGGTTTGTCCATATTTAACCCAATGCTGGGTTAGGACAAACAGAGTGGATATTATAAGTAACACACTTATGTCAATTAGATAATAATTTAACACAGATGAGAAATCTGCTGCTGCAAGACAGGATAATTGGTCAATGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34120

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000022139	Essential Splice Site	166	263	None	7

The following genes are also affected by this mutation:

ENSDARG00000090428

Genomic Location (Zv9):

Chromosome 7 (position 36524035)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	34797878
GRCz11	7	35069355

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCATTTTCTTTCGTGCAAGCTTTCAAACACATTTTTGTAACTTTTTTTT[A/T]GCTCCTGATACCCCTGCCCTGCTCCAGCAGGCCGCTCTGCCTCTGCTGAC

Long Flanking Sequence:

CTGCTGCAAGACAGGATAATTGGTCAATGGAATGCTTACATGTCCATATTTTCTTTACAAAGGTTTTCAAGCATCCTAATTTCAACATGTTCACCATCAACAATGACATCCTGCTGATCAAGCTGGCCACTCCTGCTAAGATCAACACTCATGTGTCTCCTGTGTGTCTCGCCGAGACCAACGACAACTTCCCTGGTGGCATGAAGTGTGTGACCTCCGGATGGGGCCTGACCAAACACAATGGTATAAATATTTTCAAAATTTGAGTCACATTTATTATCTTATCTGTAAAAATGAAAGTTTGGTGGTTTAAAATTGTATAAATATGTAATCATATTTTTTATGCTTACTGTATAATATTTCATTGTATGCATAACATATCTTTATGTTACCATATTTCAAACTTAACCTTTTTAGGTTAATTATCCAATTAATTCTCTATAATCGTGAATCATTTTCTTTCGTGCAAGCTTTCAAACACATTTTTGTAACTTTTTTTT[A/T]GCTCCTGATACCCCTGCCCTGCTCCAGCAGGCCGCTCTGCCTCTGCTGACCAATGAAGACTGCAAACGCTTCTGGGGAAACAAAATCACTGATCTAATGGTCTGTGCTGGAGCATCTGGTGCTTCTTCCTGCATGGTAAGTCCTTCTGTTTTTCTCAGTTTACCTCTCTATTTGTCAAGTTTTCAAACACGGTATATATCTGACTTATATTTTGCCTGTTTCAGGGTGACTCTGGTGGTCCTCTGGTGTGTCAGAAAGATGGAGTCTGGACTCTGGTTGGTATCGTGTCCTGGGGTAGCAGCGTTTGCTCCACCAGTTCTCCCGGTGTTTACGCCCGCGTCACCAAGCTCCGTGCCTGGGTTGACCAGACCATCACTGCAAACTAAATCACCAAGCTAATGTTCATGGTCATAATGTTCATCAATAAAGCTTTATTTTGAAAAAAAAGAAAACACCCTGCTTGTTATTATGCTTTAAAGTAATTTACAATAGACATTTAA

Associated Phenotype:

Not determined